These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 10653763)

  • 21. Development of a rapid quantitative PCR assay for direct detection and quantification of culturable and non-culturable Escherichia coli from agriculture watersheds.
    Khan IU; Gannon V; Kent R; Koning W; Lapen DR; Miller J; Neumann N; Phillips R; Robertson W; Topp E; van Bochove E; Edge TA
    J Microbiol Methods; 2007 Jun; 69(3):480-8. PubMed ID: 17433480
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Simultaneous detection of enteric bacteria from surface waters by QPCR in comparison with conventional bacterial indicators.
    Liu YJ; Zhang CM; Wang XC
    Environ Monit Assess; 2009 Nov; 158(1-4):535-44. PubMed ID: 18931927
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The PCR amplification of non-tuberculous mycobacterial 16S rRNA sequences from soil.
    Mendum TA; Chilima BZ; Hirsch PR
    FEMS Microbiol Lett; 2000 Apr; 185(2):189-92. PubMed ID: 10754246
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Enumeration of total bacteria and bacteria with genes for proteolytic activity in pure cultures and in environmental samples by quantitative PCR mediated amplification.
    Bach HJ; Tomanova J; Schloter M; Munch JC
    J Microbiol Methods; 2002 May; 49(3):235-45. PubMed ID: 11869788
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A new approach to utilize PCR-single-strand-conformation polymorphism for 16S rRNA gene-based microbial community analysis.
    Schwieger F; Tebbe CC
    Appl Environ Microbiol; 1998 Dec; 64(12):4870-6. PubMed ID: 9835576
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Detection of fecal bacteria and source tracking identifiers in environmental waters using rRNA-based RT-qPCR and rDNA-based qPCR assays.
    Pitkänen T; Ryu H; Elk M; Hokajärvi AM; Siponen S; Vepsäläinen A; Räsänen P; Santo Domingo JW
    Environ Sci Technol; 2013; 47(23):13611-20. PubMed ID: 24187936
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Development of oligonucleotide primers for the specific PCR-based detection of the most frequent Enterobacteriaceae species DNA using wec gene templates.
    Bayardelle P; Zafarullah M
    Can J Microbiol; 2002 Feb; 48(2):113-22. PubMed ID: 11958564
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Effect of primer mismatch, annealing temperature and PCR cycle number on 16S rRNA gene-targetting bacterial community analysis.
    Sipos R; Székely AJ; Palatinszky M; Révész S; Márialigeti K; Nikolausz M
    FEMS Microbiol Ecol; 2007 May; 60(2):341-50. PubMed ID: 17343679
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Source tracking of Escherichia coli by 16S-23S intergenic spacer region denaturing gradient gel electrophoresis (DGGE) of the rrnB ribosomal operon.
    D'Elia TV; Cooper CR; Johnston CG
    Can J Microbiol; 2007 Oct; 53(10):1174-84. PubMed ID: 18026210
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Acinetobacter diversity in environmental samples assessed by 16S rRNA gene PCR-DGGE fingerprinting.
    Vanbroekhoven K; Ryngaert A; Wattiau P; Mot R; Springael D
    FEMS Microbiol Ecol; 2004 Oct; 50(1):37-50. PubMed ID: 19712375
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genus- and species-specific PCR-based detection of dairy propionibacteria in environmental samples by using primers targeted to the genes encoding 16S rRNA.
    Rossi F; Torriani S; Dellaglio F
    Appl Environ Microbiol; 1999 Sep; 65(9):4241-4. PubMed ID: 10473444
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Comparison of quantitative PCR assays for Escherichia coli targeting ribosomal RNA and single copy genes.
    Chern EC; Siefring S; Paar J; Doolittle M; Haugland RA
    Lett Appl Microbiol; 2011 Mar; 52(3):298-306. PubMed ID: 21204885
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Real-time quantitative broad-range PCR assay for detection of the 16S rRNA gene followed by sequencing for species identification.
    Zucol F; Ammann RA; Berger C; Aebi C; Altwegg M; Niggli FK; Nadal D
    J Clin Microbiol; 2006 Aug; 44(8):2750-9. PubMed ID: 16891488
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Rapid identification of Riemerella anatipestifer on the basis of specific PCR amplifying 16S rDNA].
    Qu FF; Cai C; Zheng XJ; Zhang DB
    Wei Sheng Wu Xue Bao; 2006 Feb; 46(1):13-7. PubMed ID: 16579457
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Application of multiplex semi-nested polymerase chain reaction in detection of pathogens in cerebrospinal fluid].
    Yan ZY; Wang B; Bi CX
    Zhonghua Liu Xing Bing Xue Za Zhi; 2003 Apr; 24(4):296-9. PubMed ID: 12820949
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Detection of enteric pathogenic bacteria from surface waters by quantitative polymerase chain reaction (QPCR)].
    Liu YJ; Zhang CM; Wang XC; Lü YJ; Zuo LL
    Huan Jing Ke Xue; 2008 May; 29(5):1175-80. PubMed ID: 18624175
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Nonspecific PCR amplification of the 16S rRNA gene segment in different bacteria by use of primers specific for Campylobacter, Arcobacter, and Helicobacter spp.
    Raut AD; Kapadnis BP; Shashidhar R; Bandekar JR; Vaishampayan P; Shouche YS
    J Clin Microbiol; 2007 Apr; 45(4):1376-7. PubMed ID: 17403769
    [No Abstract]   [Full Text] [Related]  

  • 38. Bias caused by template annealing in the amplification of mixtures of 16S rRNA genes by PCR.
    Suzuki MT; Giovannoni SJ
    Appl Environ Microbiol; 1996 Feb; 62(2):625-30. PubMed ID: 8593063
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A highly selective PCR protocol for detecting 16S rRNA genes of the genus Pseudomonas (sensu stricto) in environmental samples.
    Widmer F; Seidler RJ; Gillevet PM; Watrud LS; Di Giovanni GD
    Appl Environ Microbiol; 1998 Jul; 64(7):2545-53. PubMed ID: 9647828
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PCR primers designed from malic acid dehydrogenase gene and their use for detection of Escherichia coli in water and milk samples.
    Hsu SC; Tsen HY
    Int J Food Microbiol; 2001 Feb; 64(1-2):1-11. PubMed ID: 11252491
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.